optic atrophy
disorder characterized by loss of optic nerve fibers. It may be inherited or acquired. Acquired causes include ischemia, optic nerve neuropathy, glaucoma, trauma, radiation, brain tumors, and multiple sclerosis. It leads to vision disturbances
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optic atrophy
Summary
optic atrophy is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- optic atrophy's instance of is recorded as rare disease[3].
- optic atrophy's instance of is recorded as class of disease[4].
- optic atrophy is a type of optic nerve disease[5].
- optic atrophy is a type of atrophy[6].
- optic atrophy is a type of disease[7].
- optic atrophy's ICD-9-CM is recorded as 377.1[8].
- optic atrophy's ICD-9-CM is recorded as 377.10[9].
- optic atrophy's NCI Thesaurus ID is recorded as C34863[10].
- optic atrophy's health specialty is recorded as neurology[11].
- optic atrophy's genetic association is recorded as OPA3[12].
- optic atrophy's genetic association is recorded as DNM1L[13].
- optic atrophy's genetic association is recorded as OPA1[14].
- optic atrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_5723[15].
- optic atrophy's exact match is recorded as http://identifiers.org/doid/DOID:5723[16].
- optic atrophy's exact match is recorded as http://purl.obolibrary.org/obo/HP_0000648[17].
- optic atrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98673[18].
- optic atrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
optic atrophy is known by 5 alternative names across languages and contexts.[2]